Deeper Insight into the Diels-Alder Reaction through the Activation Strain Model

被引:52
作者
Fernandez, Israel [1 ]
Bickelhaupt, F. Matthias [2 ,3 ,4 ]
机构
[1] Univ Complutense Madrid, Dept Quim Organ 1, Ciudad Univ, E-28040 Madrid, Spain
[2] Vrije Univ Amsterdam, Dept Theoret Chem, De Boelelaan 1083, NL-1081 HV Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, ACMM, De Boelelaan 1083, NL-1081 HV Amsterdam, Netherlands
[4] Radboud Univ Nijmegen, Inst Mol & Mat, Heyendaalseweg 135, NL-6525 AJ Nijmegen, Netherlands
关键词
activation strain model; chemical reactivity; cycloaddition; Diels-Alder; energy decomposition analysis; selectivity; POLYCYCLIC AROMATIC-HYDROCARBONS; SECONDARY ORBITAL INTERACTIONS; WALLED CARBON NANOTUBES; HYPERCONJUGATIVE AROMATICITY; ADDITION-REACTIONS; STERIC COURSE; CYCLOADDITIONS; DISTORTION/INTERACTION; 1,3-DIPOLAR; DIENES;
D O I
10.1002/asia.201601203
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this Focus Review, we present the application of the so-called Activation Strain Model of chemical reactivity to the Diels-Alder cycloaddition reaction. To this end, representative recent examples have been selected to illustrate the power of this new computational approach to gain a deeper quantitative understanding of this fundamental process in chemistry. We cover a wide range of issues, such as, the "endo-rule", reactivity trends emerging from systematic variation in the reactants' strain, and cycloaddition reactions involving relevant species in material science, that is, fullerenes, polycyclic aromatic hydrocarbons and nanotubes.
引用
收藏
页码:3297 / 3304
页数:8
相关论文
共 50 条
  • [41] The Diels-Alder reaction: doomed to academic praise only?
    Seghers, Sofie
    Thybaut, Joris W.
    Stevens, Christian, V
    CHIMICA OGGI-CHEMISTRY TODAY, 2018, 36 (02) : 40 - 43
  • [42] New Insights into the Diels-Alder Reaction of Graphene Oxide
    Brisebois, Patrick P.
    Kuss, Christian
    Schougaard, Steen B.
    Izquierdo, Ricardo
    Siaj, Mohamed
    CHEMISTRY-A EUROPEAN JOURNAL, 2016, 22 (17) : 5849 - 5852
  • [43] Intramolecular Diels-Alder reactions. 5 - Facile synthesis of an octahydrobenzocycloheptenone derivative utilising intramolecular Diels-Alder reaction
    Frey, B
    Reissig, HU
    JOURNAL FUR PRAKTISCHE CHEMIE-CHEMIKER-ZEITUNG, 1999, 341 (02): : 173 - 178
  • [44] The Role of Supramolecular Intermediates in the Potential Energy Surface of the Diels-Alder Reaction
    Ramirez-Gualito, Karla
    Lopez-Mora, Nestor
    Jimenez-Vazquez, Hugo A.
    Tamariz, Joaquin
    Cuevas, Gabriel
    JOURNAL OF THE MEXICAN CHEMICAL SOCIETY, 2013, 57 (04) : 267 - 275
  • [45] An Effective Diels-Alder Reaction of Vinyl Allenols with Dienophiles
    Choi, Subin
    Hwang, Hoon
    Lee, Phil Ho
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2011, 2011 (07) : 1351 - 1356
  • [46] The Diels-Alder Reaction for the Synthesis of Polycyclic Aromatic Compounds
    Dyan, Ok Ton
    Borodkin, Gennady I.
    Zaikin, Pavel A.
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2019, 2019 (44) : 7271 - 7306
  • [47] Computational design of a lipase for catalysis of the Diels-Alder reaction
    Linder, Mats
    Hermansson, Anders
    Liebeschuetz, John
    Brinck, Tore
    JOURNAL OF MOLECULAR MODELING, 2011, 17 (04) : 833 - 849
  • [48] A mechanochemical study of the effects of compression on a Diels-Alder reaction
    Jha, Sanjiv K.
    Brown, Katie
    Todde, Guido
    Subramanian, Gopinath
    JOURNAL OF CHEMICAL PHYSICS, 2016, 145 (07)
  • [49] REACTION PREDICTION BY THE BEPPE PROGRAM - THE DIELS-ALDER CYCLOADDITION
    SELLO, G
    JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, 1995, 340 : 29 - 43
  • [50] Computational design of a lipase for catalysis of the Diels-Alder reaction
    Mats Linder
    Anders Hermansson
    John Liebeschuetz
    Tore Brinck
    Journal of Molecular Modeling, 2011, 17 : 833 - 849